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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72238Generated: October 25, 2026

Diisopropylamine → 5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/72238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant1-PiperidinecarboxaldehydeHCID 17429—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 2805185—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl esterHCID 57618725—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1.6M n-BuLi solution in hexane (12 mL) was added dropwise to a solution of diisopropylamine (2.9 mL) in THF (30 mL) at −78° C. The reaction mixture was stirred at 0° C. for 10 min and then cooled to −78° C., and a solution of 3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester (1.5 g) in THF (15 mL) was added. The reaction mixture was stirred at −78° C. for 30 min and then 1-formylpiperidine (4 g) was added, and the mixture was again stirred at this temperature for 1.5 h. Subsequently, saturated ammonium chloride solution was added and the reaction mixture was allowed to reach room temperature. The aqueous phase was extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulfate and the solvent was removed in vacuo. The product with the molecular weight of 281.0 (C9H6F3NO4S) was obtained in this way; MS (ESI): 282 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828991B2
Source datasetuspto-grants-2014_09
ORD IDord-063af6f49cc04f6fbaaa08dfff6a4a13
Source noteuspto-grants-2014_09